Variant: rs369675346 

    present in Gene: CNTNAP2
    present in Chromosome: 7
    Position on Chromosome: 147120974
    Alleles of this Variant: C/A;T

rs369675346 in CNTNAP2 gene and Epilepsy, Rolandic PMID 29358611 2018 Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.